Gene >> INVS
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262457 |
| Start |
100229761:100229761(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.549G>T |
| AA Mutation |
p.Lys183Asn(p.K183N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262457 |
| Start |
100273033:100273033(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1741C>A |
| AA Mutation |
p.Leu581Ile(p.L581I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |